| S.N. | Purchaser’s Specifications |
| 1 | Patient Monitor, 5 parameter |
| Name of Bidder | |
| Manufacturer | |
| Brand | |
| Type / Model | |
| Country of Origin | |
| 2 | Description of Function |
| 2.1 | It should be suitable for usage in Emergency, Operation Room and ICU Capable of monitoring ECG, SPO2, Non Invasive Blood Pressure (NIBP), Respiration Rate and Temperature. |
| 3 | Operational Requirements |
| 3.1 | It shall operate on AC power supply as well as built-in battery |
| 4 | System Configuration |
| 4.1 | Five parameter Patient Monitor, portable with complete accessories |
| 5 | Technical Specifications |
| 5.1 | Monitor must be able to monitor ECG, Respiration, SpO2, NIBP and Temperature as a standard parameter. |
| 5.2 | At least 12” high resolution TFT display with LED backlight with touch screen. |
| 5.3 | Display waveform: simultaneously display of at least 10 waveforms along with related numerical parameters on single screen. |
| 5.4 | Monitor must have Lithium ion Battery. More than 3 hour battery Backup. |
| 5.5 | Should have Adult, Pediatric and neonatal measurement mode. |
| 5.6 | Shall have Protection system against defibrillator discharge. |
| 5.7 | Shall have atleast 72-hour ECG waveform data storage and recall with more than 2000 hour data trends, graphics and tabular view. |
| 5.8 | 2000 groups event, ARR and SpO2 storage |
| 5.9 | The monitor should be able to configure automatically for new parameters as they are connected. |
| 5.10 | Should have alarm indicators with different alarm tones and visible alarm lights indicators for different issues. |
| 5.11 | The key volume, alarm volume and beat volume should be adjustable according to clinical practices and/or preferences. |
| 5.1 | Shall have Integrated 3 channel thermal Printer to record the events. |
| 5.13 | Connection and interface: Should have network capability to connect central monitoring system. |
| 5.14 | Clinicians should be able to “freeze” applications at the bedside and have access to real-time ECG monitoring and other information at the same time. |
| 6 | NIB |
| 6.1 |
Technique: Oscillometric Measurement mode: Manual , Automatic and STAT |
| 6.2 | Measuring time: <30 seconds (typical adult cuff) |
| 6.3 | Measuring range: Systolic pressure: 40mmHg~275mmHg Diastolic pressure: 10mmHg~210mmHg Mean arterial pressure: 20mmHg~230mmHg |
| 7 | SpO2 |
| 7.1 | Transducer: Dual-wave length LED SpO2 measuring range: 0%~100% SpO2 measuring accuracy: 2% for range from 70% to 100% |
| 7.2 | PR measurin range: 0 to 250 bpm. Accuracy +/-2% |
| 8 | ECG |
| 8.1 | HR measuring range: 15bpm~350bpm HR measuring accuracy: ±1% or ±2bpm |
| 9 | TEMP |
| 9.1 | Measuring range : 21.0°C~50.0°C Measuring accuracy: ±0.2°C for range from 25.0°C~45.0°C |
| 10 | RESP |
| 10.1 | RR measuring range: 0rpm~120rpm RR measuring accuracy: ±5% or ±2rpm |
| 13 | Accessories, spares and consumables |
| 13.1 | All standard accessories, consumables and parts required to operate the equipment, including all standard tools and cleaning and lubrication materials, to be included in the offer. |
| 13.2 | • NIBP reusable cuffs with hose of 3 various sizes (neonate, pediatric and adult) – 1 no. each. • Spo2 Probe with extension set, various size ( Neonate, Pediatric and Adult) – 1 no each .• ECG:- 3/5 lead ECG cable and wire- 1 set• TEMP:- Skin temperature probe- 1 set |
| 14 | Operating Environment |
| 14.1 | The product offered shall be designed to be stored and to operate normally under the conditions of the purchaser’s country. The conditions include Power Supply, Climate, Temperature, Humidity, etc. |
| 14.2 | Power supply: 220 – 240 VAC, 50Hz fitted with appropriate plug. |
| 15 | Standards and Safety Requirements |
| 15.1 | Must submit ISO13485:2003/AC:2007 for Medical Devices AND |
| 15.0 | Must Submit CE (93/42 EEC) Directive certificate and USFDA approved product certificate. |
| 15.4 | Shall meet IEC 61010-2-081 safety requirements for electrical equipment. |
| 16 | User Training |
| 16.1 | Must provide user training (including how to use and maintain the equipment). |
| 17 | Warranty |
| 17.1 | Comprehensive warranty for 2 years. |
| 17.2 | Maintenance Service During Warranty Period |
| 12.3 | During the warranty period supplier must ensure corrective/breakdown maintenance whenever required. (written document) |
| 18 | Installation and Commissioning |
| 18.1 | The bidder must arrange for the equipment to be installed and commissioned by certified or qualified personnel; any prerequisites for installation to be communicated to the purchaser in advance, in detail. |
| 19 | Documentation |
| 19.1 | User (Operating) manual in English. |
| 19.2 | Service (Technical / Maintenance) manual in English. |
| 19.3 | Certificate of calibration and inspection from factory. |
Technical Specification of Patient Monitor 7 Parameter
| S.N. | Purchaser’s Specifications |
| 1 | Patient Monitor, 7 parameter |
| Name of Bidder | |
| Manufacturer | |
| Brand | |
| Type / Model | |
| Country of Origin | |
| 2 | Description of Function |
| 2.1 | It should be suitable for usage in Emergency, Operation Room and ICU Capable of monitoring ECG, SPO2, Non Invasive Blood Pressure (NIBP), Respiration Rate, Etco2, 2IBP and Temperature. |
| 3 | Operational Requirements |
| 3.1 | It shall operate on AC power supply as well as built-in battery |
| 4 | System Configuration |
| 4.1 | Seven parameter Patient Monitor, portable with complete accessories |
| 5 | Technical Specifications |
| 5.1 | Monitor must be able to monitor ECG, Respiration, SpO2, NIBP, Temperature, 2IBP and EtCo2 as a standard parameter. |
| 5.2 | At least 12” high resolution TFT display with LED backlight with touch screen. |
| 5.3 | Display waveform: simultaneously display of at least 10 waveforms along with related numerical parameters on single screen. |
| 5.4 | Monitor must have Lithium ion Battery. More than 3 hour battery Backup. |
| 5.5 | Should have Adult, Pediatric and neonatal measurement mode. |
| 5.6 | Shall have Protection system against defibrillator discharge. |
| 5.7 | Shall have intelligent arrhythmia analysis and S-T segment measurement. |
| 5.8 | Shall have at least 72-hour ECG waveform data storage and recall with more than 2000 hour data trends, graphics and tabular view. |
| 5.9 | 1000 groups event, ARR and SpO2 storage |
| 5.10 | Shall have various drug calculation including oxygenation calculation, Renal function calculation, ventilation calculation, medication calculation and hemodynamic calculation. |
| 5.11 | The monitor should be able to configure automatically for new parameters as they are connected. |
| 5.1 | Should have alarm indicators with different alarm tones and visible alarm lights indicators for different issues. |
| 5.13 | The key volume, alarm volume and beat volume should be adjustable according to clinical practices and/or preferences. |
| 5.14 | Shall have Integrated 3 channel thermal Printer to record the events. |
| 5.15 | Connection and interface: Should have network capability to connect central monitoring system. |
| 5.16 | Clinicians will be able to “freeze” applications at the bedside and have access to real-time ECG monitoring and other information at the same time. |
| 6 | NIB |
| 6.1 | Technique: Oscillometric Measurement mode: Manual , Automatic and STAT |
| 6.2 | Measuring time: <30 seconds (typical adult cuff) |
| 6.3 | Measuring range: Systolic pressure: 40mmHg~275mmHg Diastolic pressure: 10mmHg~210mmHg Mean arterial pressure: 20mmHg~230mmHg |
| 7 | SpO2 |
| 7.1 | Transducer: Dual-wave length LED SpO2 measuring range: 0%~100% SpO2 measuring accuracy: 2% for range from 70% to 100% |
| 7.2 | PR measuring range: 0 to 250 bpm. Accuracy +/-2% |
| 8 | ECG |
| 8.1 | HR measuring range: 15bpm~350bpm HR measuring accuracy: ±1% or ±2bpm |
| 9 | TEMP |
| 9.1 | Measuring range : 21.0°C~50.0°C Measuring accuracy: ±0.2°C for range from 25.0°C~45.0°C |
| 10 | RESP |
| 10.1 | RR measuring range: 0rpm~120rpm RR measuring accuracy: ±5% or ±2rpm |
| 11 | Etco2 |
| 11.1 | Side Stream or main stream. |
| 12 | IBP |
| 12.1 | Dual channel IBP. |
| 13 | Accessories, spares and consumables |
| 13.1 | All standard accessories, consumables and parts required to operate the equipment, including all standard tools and cleaning and lubrication materials, to be included in the offer. |
| 13.2 | • NIBP reusable cuffs with hose of 3 various sizes (neonate, children and adult) – 1 no. each. • Spo2 Probe with extension set, various size ( Neonate, Pedriac and Adult) – 1 no each .• ECG:- 3/5 lead ECG cable and wire- 1 set • TEMP:- Skin temperature probe- 1 set • IBP module:- 2 sets of cables with 4 sets of kits • Artema Side-stream EtCO2 module:- Side-stream EtCO2 kit- 1 set |
| 14 | Operating Environment |
| 14.1 | The product offered shall be designed to be stored and to operate normally under the conditions of the purchaser’s country. The conditions include Power Supply, Climate, Temperature, Humidity, etc. |
| 14.2 | Power supply: 220 – 240 VAC, 50Hz fitted with appropriate plug. |
| 15 | Standards and Safety Requirements |
| 15.1 | Must submit ISO13485:2003/AC:2007 for Medical Devices AND |
| 15.0 | Must Submit CE (93/42 EEC) Directive certificate and USFDA approved product certificate. |
| 15.4 | Shall meet IEC 61010-2-081 safety requirements for electrical equipment. |
| 16 | User Training |
| 16.1 | Must provide user training (including how to use and maintain the equipment). |
| 17 | Warranty |
| 17.1 | Comprehensive warranty for 2 years. |
| 17.2 | Maintenance Service During Warranty Period |
| 12.3 | During the warranty period supplier must ensure corrective/breakdown maintenance whenever required. (written document) |
| 18 | Installation and Commissioning |
| 18.1 | The bidder must arrange for the equipment to be installed and commissioned by certified or qualified personnel; any prerequisites for installation to be communicated to the purchaser in advance, in detail. |
| 19 | Documentation |
| 19.1 | User (Operating) manual in English. |
| 19.2 | Service (Technical / Maintenance) manual in English. |
| 19.3 | Certificate of calibration and inspection from factory. |